338362
2,3,4-三氟硝基苯
99%
别名:
1,2,3-三氟-4-硝基苯, 4-硝基-1,2,3-三氟苯
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关于此项目
线性分子式:
F3C6H2NO2
化学文摘社编号:
分子量:
177.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-238-4
MDL number:
Assay:
99%
Form:
liquid
产品名称
2,3,4-三氟硝基苯, 99%
InChI key
ARCACZWMYGILNI-UHFFFAOYSA-N
InChI
1S/C6H2F3NO2/c7-3-1-2-4(10(11)12)6(9)5(3)8/h1-2H
SMILES string
[O-][N+](=O)c1ccc(F)c(F)c1F
assay
99%
form
liquid
refractive index
n20/D 1.492 (lit.)
bp
92 °C/20 mmHg (lit.)
density
1.541 g/mL at 25 °C (lit.)
functional group
fluoro
nitro
Application
2,3,4-Trifluoronitrobenzene was employed as starting reagent in the synthesis of ofloxacin. It was also used in the synthesis of the third generation quinolones antibacterial drugs.
General description
2,3,4-Trifluoronitrobenzene is a fluoronitrobenzene and its biotransformation under methanogenic conditions has been studied by semicontinuous and batch tests. 2,3,4-Trifluoronitrobenzene is an important pharmaceutical intermediate.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
199.4 °F - closed cup
flash_point_c
93 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Analytical profile of the fluoroquinolone antibacterials. I. Ofloxacin.
Okeri HA and Arhewoh IM.
African Journal of Biotechnology, 7(6) (2008)
Ultrasonic Promoted in Synthesis of 2, 3, 4-trichloronitrobenzene [J].
Yunqiang L and Guohui C.
Guangzhou Chemical Industry/ Guangzhou Huagong, 3, 024-024 (2009)
Zhiqing Zhao et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 49(10), 1187-1197 (2014-05-23)
The fluorinated compounds are becoming a ubiquitous class of environmental contaminants because of their widespread applications, and their fate is a matter of great concern under anaerobic environment. In this work, the biotransformation of five fluoronitrobenzenes (FNBs), i.e., 2-fluoronitrobenzene (2-FNB)
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